GlyCosmos Portal

Caenorhabditis elegans

Summary

Taxonomy ID: 6239
PubChem Taxonomy: 6239

Genes (186) Glycans (3) Glycoproteins (1454) Lectins (39) Pathways (499)

Displaying entries **1 - 25** of **186** in total

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Gene ID	Gene Name ▼	Gene Symbol	Disease Ontology
187700	putative sugar kinase R08D7.7	R08D7.7
178364	putative phosphomannomutase	F52B11.2	congenital disorder of glycosylation Ia congenital disorder of glycosylation type I congenital disorder of glycosylation
171965	putative phosphoglycerate kinase	pgk-1	Parkinson's disease cancer hemolytic anemia phosphoglycerate kinase 1 deficiency
176388	putative mannose-6-phosphate isomerase	ZK632.4	carbohydrate metabolic disorder congenital disorder of glycosylation Ib congenital disorder of glycosylation type I
172509	putative glycerol-3-phosphate dehydrogenase, mitochondrial	gpdh-3	type 2 diabetes mellitus
173747	putative glycerol kinase	R11F4.1	familial hypercholesterolemia glycerol kinase deficiency
176760	putative glucosamine-6-phosphate isomerase	T03F6.3
175506	putative galactose-1-phosphate uridylyltransferase	ZK1058.3	classic galactosemia galactosemia
180628	putative endochitinase	cht-1	acute myeloid leukemia arteriosclerosis asthma bacterial meningitis breast cancer bronchopulmonary dysplasia chondrosarcoma chronic obstructive pulmonary disease colorectal carcinoma congestive heart failure coronary artery disease cryptococcosis endometrial cancer glioblastoma hypertension lung non-small cell carcinoma melanoma multiple myeloma myocardial infarction ovarian cancer pre-eclampsia prostate carcinoma pulmonary fibrosis pulmonary sarcoidosis rheumatoid arthritis schizophrenia silicosis sinusitis small cell carcinoma systemic scleroderma temporal arteritis type 1 diabetes mellitus type 2 diabetes mellitus
182392	putative dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase	algn-6	congenital disorder of glycosylation Ic congenital disorder of glycosylation type I
174542	putative dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase	algn-8	congenital disorder of glycosylation Ih congenital disorder of glycosylation type I polycystic liver disease
176437	putative citrate synthase, mitochondrial	cts-1	bipolar disorder congestive heart failure dilated cardiomyopathy hyperthyroidism hypertrophic cardiomyopathy hypothyroidism limb ischemia myocardial infarction retinal degeneration
181517	putative beta-mannosidase	C33G3.4	beta-mannosidosis
176557	putative N-acetylgalactosaminyltransferase 9	gly-9
179185	putative Dol-P-Man:Man(7)GlcNAc(2)-PP-Dol alpha-1,6-mannosyltransferase	algn-12	congenital disorder of glycosylation Ig congenital disorder of glycosylation type I
173393	putative ADP-dependent glucokinase	C50D2.7
174386	phosphatidylinositol N-acetylglucosaminyltransferase	piga-1	autosomal recessive congenital ichthyosis 4B multiple congenital anomalies-hypotonia-seizures syndrome 2 paroxysmal nocturnal hemoglobinuria
180119	glycogenin glucosyltransferase	gyg-2	glycogen storage disease XV glycogen storage disease
187799	glucuronosyltransferase	ugt-59
174705	Zinc finger transcription factor pqm-1	pqm-1
190099	Xylosyltransferase sqv-6;protein xylosyltransferase	sqv-6	Desbuquois dysplasia kidney disease polycystic kidney disease pseudoxanthoma elasticum type 1 diabetes mellitus
176382	Xylosylprotein 4-beta-galactosyltransferase	sqv-3	Ehlers-Danlos syndrome spondylodysplastic type 1 Ehlers-Danlos syndrome
176077	Uridine and thymidine phosphorylase	upp-1	middle cerebral artery infarction
176633	Uracil-DNA glycosylase	ung-1	dysgammaglobulinemia immunodeficiency with hyper IgM type 5
174243	Uncharacterized protein	B0495.5	oligoasthenoteratozoospermia

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